Needham & Company LLC reaffirmed their buy rating on shares of Taysha Gene Therapies (NASDAQ:TSHA – Free Report) in a report issued on Tuesday,Benzinga reports. Needham & Company LLC currently has a $6.00 price objective on the stock.
Several other equities analysts also recently commented on the stock. Chardan Capital reiterated a “buy” rating and issued a $7.00 price objective on shares of Taysha Gene Therapies in a report on Tuesday, August 13th. Canaccord Genuity Group decreased their price target on shares of Taysha Gene Therapies from $7.00 to $6.00 and set a “buy” rating on the stock in a research note on Wednesday, August 14th. Eight research analysts have rated the stock with a buy rating, According to MarketBeat.com, Taysha Gene Therapies presently has a consensus rating of “Buy” and a consensus target price of $6.63.
Read Our Latest Stock Report on Taysha Gene Therapies
Taysha Gene Therapies Stock Performance
Institutional Inflows and Outflows
Several hedge funds have recently made changes to their positions in TSHA. Creative Planning acquired a new stake in Taysha Gene Therapies during the third quarter worth approximately $28,000. Principal Financial Group Inc. acquired a new position in Taysha Gene Therapies in the second quarter valued at about $48,000. China Universal Asset Management Co. Ltd. lifted its holdings in shares of Taysha Gene Therapies by 79.4% during the 3rd quarter. China Universal Asset Management Co. Ltd. now owns 39,417 shares of the company’s stock worth $79,000 after acquiring an additional 17,446 shares during the period. Intech Investment Management LLC acquired a new position in shares of Taysha Gene Therapies during the 3rd quarter worth $85,000. Finally, Scientech Research LLC bought a new position in shares of Taysha Gene Therapies in the second quarter worth about $97,000. 77.70% of the stock is owned by institutional investors.
Taysha Gene Therapies Company Profile
Taysha Gene Therapies, Inc, a gene therapy company, focuses on developing and commercializing adeno-associated virus-based gene therapies for the treatment of monogenic diseases of the central nervous system. It primarily develops TSHA-120 for the treatment of giant axonal neuropathy; TSHA-102 for the treatment of Rett syndrome; TSHA-121 for the treatment of CLN7 disease; TSHA-118 for the treatment of CLN1 disease; TSHA-105 for the treatment of for SLC13A5 deficiency; TSHA-113 for the treatment of tauopathies; TSHA-106 for the treatment of angelman syndrome; TSHA-114 for the treatment of fragile X syndrome; and TSHA-101 for the treatment of GM2 gangliosidosis.
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